US4126572A - Built liquid detergent composition - Google Patents

Built liquid detergent composition Download PDF

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US4126572A
US4126572A US05/773,863 US77386377A US4126572A US 4126572 A US4126572 A US 4126572A US 77386377 A US77386377 A US 77386377A US 4126572 A US4126572 A US 4126572A
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sodium
phosphonic acid
potassium
acid
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US05/773,863
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Ho Tan Tai
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Lever Brothers Co
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Lever Brothers Co
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/34—Organic compounds containing sulfur
    • C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/83—Mixtures of non-ionic with anionic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/36—Organic compounds containing phosphorus
    • C11D3/361—Phosphonates, phosphinates or phosphonites

Definitions

  • the present invention relates to an aqueous built liquid detergent composition. More particularly it relates to an improvement in the storage stability of aqueous built liquid detergent compositions, obtained by the inclusion of a particular hydrotrope system therein.
  • aqueous built liquid detergent compositions may suffer from storage instability leading to phase-separation, both at room temperature and at temperatures below 0° C., if no proper precautions have been taken. Furthermore, aqueous built liquid detergent compositions are normally required to be homogeneous, clear liquids, which also demands special precautions.
  • hydrotropes such as urea, ethyl-alcohol, toluene-, cumene- and xylene sulphonates.
  • hydrotropes may give the desired effects, the amount required may be rather high, or, with particular aqueous built liquid detergent compositions, they may not produce the required degree of homogeneity, clarity and storage stability.
  • hydrotrope system comprising a sulphonate-type hydrotrope of the general formula ##STR1## in which R is a methyl, dimethyl or isopropyl residue and M ⁇ H, NH 4 , substituted NH 4 , or an alkali metal, such as sodium or potassium, and an alkane phosphonic acid of the general formula ##STR2## in which R is a saturated alkyl residue with 4-10 carbon atoms, and M is H, NH 4 , substituted NH 4 or an alkali metal such as sodium or potassium, significantly improves the homogeneity, clarity and storage stability of built aqueous liquid detergents.
  • the combination enables a significant reduction of the amount of sulphonate-type hydrotrope used, while simultaneously improving the overall hydrotrope effect, and vice versa with regard to the alkane-phosphonic acid alone.
  • the sulphonate-type hydrotropes are toluene-, xylene- and cumene sulphonates, preferably in the form of the sodium salts, although potassium, ammonium and substituted ammonium salts may also be used if desired. Particularly preferred are sodium toluene- and xylene sulphonate.
  • the other hydrotrope is a monoalkane phosphonic acid, in which the alkane residue may be branched-, but is preferably straight-chained, and contains from 4-10 carbon atoms. It may be used in the acid form, or in the form of the mono- or dialkali metal metal such as sodium or potassium, ammonium and substituted ammonium salt. Particularly preferred is monooctane phosphonic acid.
  • the amount of the sulphonate-type hydrotrope used in the present invention is from 0.75-8.5% by weight of the composition, and the amount of monoalkane phosphonic acid is from 0.5-2.5%, preferably 1-2% by weight of the composition, with the proviso that in the case of sodium xylene sulphonate more than 4% thereof should be used if the amount of monoalkane phosphonic acid is 1% or less.
  • the hydrotrope system provides for better stability, clarity and homogeneity when included in aqueous built liquid detergent compositions, i.e. compositions containing an active synthetic detergent composition and an inorganic builder salt.
  • Such builder salts include the sodium or potassium ortho-, pyro- and polyphosphates, and sodium or potassium carbonates, and mixtures thereof.
  • aqueous liquid detergent compositions which contain alkali metal carbonates such as sodium or potassium carbonate as the builder salt.
  • alkali metal carbonates such as sodium or potassium carbonate
  • the amount of the inorganic builder salt present in such liquids may vary from 1-25% by weight, and preferably lies between 5 and 15% by weight.
  • polyelectrolyte In carbonate-built liquid detergents it is useful to include a polyelectrolyte to prevent undesired incrustation or soil redeposition.
  • polyelectrolytes are e.g. polyacrylates, copolymers or ethylene with maleic anhydride or copolymers of maleic anhydride with vinylmethylether.
  • Particularly preferred are polyacrylic acids with a molecular weight of between 3,500-22,000.
  • the amount of polyelectrolyte used varies from 0.5-5%, preferably from 1-3% by weight.
  • liquid detergent compositions may comprise a simple synthetic detergent active such as an alkylaryl sulphonate with 10-24 carbon atoms in the alkyl chain, an alkane sulphonate with 10-24 carbon atoms in the alkane chain, alkylether sulphates with 10-24 carbon atoms in the alkyl chain and from 1-10 moles of an alkylene oxide such as ethylene oxide and/or propylene oxide, nonionic synthetic detergents i.e.
  • a simple synthetic detergent active such as an alkylaryl sulphonate with 10-24 carbon atoms in the alkyl chain
  • an alkane sulphonate with 10-24 carbon atoms in the alkane chain
  • alkylether sulphates with 10-24 carbon atoms in the alkyl chain and from 1-10 moles of an alkylene oxide such as ethylene oxide and/or propylene oxide
  • nonionic synthetic detergents i.e.
  • an aqueous built liquid detergent composition which comprises a ternary system of detergent active materials, i.e. an anionic + a nonionic + a soap.
  • the anionic synthetic detergent is a C 10 -C 24 alkylbenzene sulphonate (as alkali metal, e.g.
  • the nonionic is an ethoxylated linear C 8 -C 22 alcohol condensed with 3 to 25 moles of ethylene oxide and the soap is a sodium or potassium, ammonium or substituted ammonium salt of a polymeric fatty acid, predominantly consisting of dimerized oleic acid.
  • the amounts of the anionic, nonionic and soap may vary from 5-15, 1-5 and 1-5% respectively.
  • Other anionics, nonionics and soaps, including soaps of C 10 -C 24 fatty acids may also be used instead of the above-identified ones.
  • compositions may furthermore comprise the usual ingredients such as silicates, borates, phosphates, fluorescers, soil-suspending agents, lather controllers or lather boosters, perfumes, germicides, enzymes, opacifiers, anti-redeposition agents, and so on.
  • a liquid detergent formulation was prepared from the following ingredients
  • the products were assessed for clarity, homogeneity and stability, they being found satisfactory if the liquid was clear and homogeneous, or, in the case of the changing temperatures, if there were crystals which rapidly dissolved again or when there was only a temporary cloudiness.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

A critical mixture of a sulphonate-type hydrotrope and a monoalkane phosphonic acid or salt thereof when included in an aqueous built liquid detergent provides for an improved stability, clarity and homogeneity thereof.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to an aqueous built liquid detergent composition. More particularly it relates to an improvement in the storage stability of aqueous built liquid detergent compositions, obtained by the inclusion of a particular hydrotrope system therein.
2. Description of the Prior Art
It is well known that aqueous built liquid detergent compositions may suffer from storage instability leading to phase-separation, both at room temperature and at temperatures below 0° C., if no proper precautions have been taken. Furthermore, aqueous built liquid detergent compositions are normally required to be homogeneous, clear liquids, which also demands special precautions.
One of the common practices to achieve stable, homogeneous, clear liquids is to incorporate hydrotropes in aqueous built liquid detergent compositions, which solubilize particular ingredients in the liquid compositions. Commonly employed for said purpose are hydrotropes such as urea, ethyl-alcohol, toluene-, cumene- and xylene sulphonates. However, whereas such hydrotropes may give the desired effects, the amount required may be rather high, or, with particular aqueous built liquid detergent compositions, they may not produce the required degree of homogeneity, clarity and storage stability.
SUMMARY OF THE INVENTION
It has now been found that a hydrotrope system comprising a sulphonate-type hydrotrope of the general formula ##STR1## in which R is a methyl, dimethyl or isopropyl residue and M═H, NH4, substituted NH4, or an alkali metal, such as sodium or potassium, and an alkane phosphonic acid of the general formula ##STR2## in which R is a saturated alkyl residue with 4-10 carbon atoms, and M is H, NH4, substituted NH4 or an alkali metal such as sodium or potassium, significantly improves the homogeneity, clarity and storage stability of built aqueous liquid detergents.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
In comparison with the sulphonate-type hydrotropes alone, the combination enables a significant reduction of the amount of sulphonate-type hydrotrope used, while simultaneously improving the overall hydrotrope effect, and vice versa with regard to the alkane-phosphonic acid alone.
The sulphonate-type hydrotropes are toluene-, xylene- and cumene sulphonates, preferably in the form of the sodium salts, although potassium, ammonium and substituted ammonium salts may also be used if desired. Particularly preferred are sodium toluene- and xylene sulphonate.
The other hydrotrope is a monoalkane phosphonic acid, in which the alkane residue may be branched-, but is preferably straight-chained, and contains from 4-10 carbon atoms. It may be used in the acid form, or in the form of the mono- or dialkali metal metal such as sodium or potassium, ammonium and substituted ammonium salt. Particularly preferred is monooctane phosphonic acid.
The amount of the sulphonate-type hydrotrope used in the present invention is from 0.75-8.5% by weight of the composition, and the amount of monoalkane phosphonic acid is from 0.5-2.5%, preferably 1-2% by weight of the composition, with the proviso that in the case of sodium xylene sulphonate more than 4% thereof should be used if the amount of monoalkane phosphonic acid is 1% or less. The hydrotrope system provides for better stability, clarity and homogeneity when included in aqueous built liquid detergent compositions, i.e. compositions containing an active synthetic detergent composition and an inorganic builder salt. Such builder salts include the sodium or potassium ortho-, pyro- and polyphosphates, and sodium or potassium carbonates, and mixtures thereof.
The benefit of the invention is particularly achieved in aqueous liquid detergent compositions which contain alkali metal carbonates such as sodium or potassium carbonate as the builder salt. The amount of the inorganic builder salt present in such liquids may vary from 1-25% by weight, and preferably lies between 5 and 15% by weight.
In carbonate-built liquid detergents it is useful to include a polyelectrolyte to prevent undesired incrustation or soil redeposition. Such polyelectrolytes are e.g. polyacrylates, copolymers or ethylene with maleic anhydride or copolymers of maleic anhydride with vinylmethylether. Particularly preferred are polyacrylic acids with a molecular weight of between 3,500-22,000. The amount of polyelectrolyte used varies from 0.5-5%, preferably from 1-3% by weight.
Although the liquid detergent compositions may comprise a simple synthetic detergent active such as an alkylaryl sulphonate with 10-24 carbon atoms in the alkyl chain, an alkane sulphonate with 10-24 carbon atoms in the alkane chain, alkylether sulphates with 10-24 carbon atoms in the alkyl chain and from 1-10 moles of an alkylene oxide such as ethylene oxide and/or propylene oxide, nonionic synthetic detergents i.e. adducts of 5-30 moles of an alkylene oxide to a C10 -C24 primary or secondary alcohol, to a C9 -C18 alkylphenol, soaps, amphoteric surfactants etc, it has been found that the benefits of the invention are particularly obtained in an aqueous built liquid detergent composition which comprises a ternary system of detergent active materials, i.e. an anionic + a nonionic + a soap. The anionic synthetic detergent is a C10 -C24 alkylbenzene sulphonate (as alkali metal, e.g. sodium or potassium, ammonium or substituted ammonium salt), the nonionic is an ethoxylated linear C8 -C22 alcohol condensed with 3 to 25 moles of ethylene oxide and the soap is a sodium or potassium, ammonium or substituted ammonium salt of a polymeric fatty acid, predominantly consisting of dimerized oleic acid. The amounts of the anionic, nonionic and soap may vary from 5-15, 1-5 and 1-5% respectively. Other anionics, nonionics and soaps, including soaps of C10 -C24 fatty acids may also be used instead of the above-identified ones.
The compositions may furthermore comprise the usual ingredients such as silicates, borates, phosphates, fluorescers, soil-suspending agents, lather controllers or lather boosters, perfumes, germicides, enzymes, opacifiers, anti-redeposition agents, and so on.
The invention will now be further illustrated by the following Examples.
EXAMPLE I
A liquid detergent formulation was prepared from the following ingredients
______________________________________                                    
                       % by weight                                        
______________________________________                                    
dodecylbenzene sulphonic acid                                             
                         6.5                                              
dimerized oleic acid     5                                                
C.sub.13 -C.sub.15 primary alcohol, condensed with                        
11 moles of ethylene oxide                                                
                         2.7                                              
polyacrylic acid (MW 3,500-5,000)                                         
                         2.0                                              
SCMC (low viscosity)     0.15                                             
sodium silicate          11                                               
potassium hydroxide      3                                                
potassium carbonate      7                                                
sodium xylene sulphonate (40.7% active)                                   
                         x                                                
monooctane phosphonic acid (100% active)                                  
                         y                                                
water                    q.s.100.                                         
______________________________________
First a premix of the potassium hydroxide, the dodecylbenzene sulphonic acid, the dimerized oleic acid, and the C13 -C15 primary alcohol condensed with 11 moles of ethylene oxide was prepared, to which subsequently the remaining ingredients were added under agitation, and without heating. The amount of sodium xylene sulphonate (x) and monooctane phosphonic acid (y) were varied in a series of experiments, and the physical characteristics of the liquids obtained were assessed. The following results were obtained:
______________________________________                                    
Storage temperature: room temperature                                     
______________________________________                                    
% monooctane phos-                                                        
             1       2           3                                        
phonic acid = y                                                           
% sodium xylene sul-                                                      
phonate = x  0       0           0                                        
Physical character-                                                       
istics of liquid                                                          
             2 liquid                                                     
                     1 liquid and                                         
                                 1 liquid and                             
detergent compo-                                                          
             phases  1 solid phase                                        
                                 1 solid phase                            
sition                                                                    
______________________________________                                    

______________________________________                                    
Storage temperature: A: room temperature                                  
B: -4° C                                                           
% sodium xylene                                                           
sulphonate (40.7%                                                         
           12     14      16    18    20    22                            
active material)= x                                                       
% monooctane phos-                                                        
phonic acid = y                                                           
            0      0       0     0     0     0                            
Physical charac-                                                          
teristics of                                                              
           A       two liquid  homogeneous clear                          
liquid deter-      phases      liquid                                     
gent composition                                                          
"     B         two liquid homogeneous                                    
                                  crystal                                 
                phases     clear liquid                                   
                                  formation                               
______________________________________                                    

______________________________________                                    
Storage temperature: A: room temperature                                  
B: -4° C                                                           
______________________________________                                    
% sodium xylene                                                           
sulphonate (40.7%                                                         
             7       8       10    12    14                               
active material = x                                                       
% monooctane phos-                                                        
phonic acid = y                                                           
             1       1       1     1     1                                
Physical character-                                                       
istics of liquid                                                          
            A     two liquid clear, homogeneous                           
detergent compo-  phases     liquid                                       
sition                                                                    
"        B           "          "                                         
______________________________________
This example shows that monooctane phosphonic acid alone did not produce a clear, homogeneous liquid, and that only with 18-20% sodium xylene sulphonate (40.7% active material) alone a clear, homogeneous liquid both at room temperature and at -4° C. could be obtained. The combination of these two hydrotropes with e.g. 10% of sodium xylene sulphonate (40.7% active material) and 1% monooctane phosphonic acid produced already a clear, homogeneous liquid, i.e. a reduction of the sodium xylene sulphonate by almost 50% could be obtained.
EXAMPLE II
In the same manner as in Example I the following composition was prepared.
______________________________________                                    
                        % by weight                                       
______________________________________                                    
dodecylbenzene sulphonic acid                                             
                          7                                               
C.sub.13 -C.sub.15 primary alcohol, condensed with                        
11 moles of ethylene oxide                                                
                          2.5                                             
dimerized oleic acid      3.5                                             
potassium hydroxide       3.3                                             
potassium carbonate       10                                              
alkaline silicate         4.4                                             
polyacrylic acid (M.W. 3,500-5,000)                                       
                          2                                               
SCMS (low viscosity)      0.15                                            
fluorescers               0.15                                            
sodium xylene sulphonate (SXS) (100% active)                              
                          x                                               
monooctane phosphonic acid (MOP) (100% active)                            
                          y                                               
colouring agent, perfume and water                                        
                     q.s.     100                                         
______________________________________
The following storage stabilities were assessed:
______________________________________                                    
                   6% SXS       4% SXS                                    
storage temp.                                                             
         hydrotrope                                                       
                   1% MOP       2% MOP                                    
______________________________________                                    
 37° C  clear liquid clear liquid                                  
 20° C  "            "                                             
-4° C   "            "                                             
______________________________________
EXAMPLE III
Replacing potassium carbonate by sodium carbonate in Example I produces similar results, as does replacing sodium xylene sulphonate by sodium toluene- or cumene sulphonate.
EXAMPLE IV
The following two built liquid detergents were prepared:
______________________________________                                    
                       % by weight                                        
                       A     B                                            
______________________________________                                    
potassium dodecylbenzene sulphonic acid                                   
                         6.4     7.2                                      
dimerized oleic acid      5.67   5.9                                      
C.sub.13 -C.sub.15 primary alcohol, condensed with                        
11 moles of ethylene oxide                                                
                          2.65    0.77                                    
C.sub.16 -C.sub.20 linear primary alcohol, con-                           
densed with 25 moles of ethylene oxide                                    
                         --       1.35                                    
sodium tripolyphosphate  --      11.65                                    
potassium carbonate      7.0     3.9                                      
potassium orthophosphate --       1.95                                    
sodium silicate (SiO.sub.2 :Na.sub.2 O = 2)                               
                         4.3     2.9                                      
potassium hydroxide (to neutralize the                                    
dimerized oleic acid)    1.8     0.7                                      
sodium xylene sulphonate (40.7% active)                                   
                         x       x                                        
sodium toluene sulphonate (45% active)                                    
                         y       y                                        
monooctance phosphonic acid (100% active)                                 
                         z       z                                        
potassium polyacrylate   2.0      0.49                                    
sodium carboxymethylcellulose                                             
                          0.15   --                                       
water                    q.s.    q.s.                                     
______________________________________
Varying amounts of x, y and z were used (x = 0-30%, y = 0-30%, z = 0-3%), and the liquids were stored at room temperature, and at changing temperatures (-4° C. and room temperature) 5 times, each for 48 hours. The products were assessed for clarity, homogeneity and stability, they being found satisfactory if the liquid was clear and homogeneous, or, in the case of the changing temperatures, if there were crystals which rapidly dissolved again or when there was only a temporary cloudiness.
The following results were obtained:
______________________________________                                    
Liquid A was satisfactory when                                            
                      x = 10-20%                                          
                      z = 1%                                              
or                    y = 2-10%                                           
                      z = 2%                                              
Liquid B was satisfactory when                                            
                      x = 12-14%                                          
                      z = 1%                                              
or                    x = 2-10% - z = 2%                                  
or                    y = 10-12%                                          
                      z = 1%                                              
or                    y = 2-6%                                            
                      z = 2%.                                             
______________________________________
In all other cases, using x or y or z alone much more was needed to obtain satisfactory liquids, e.g. for liquid A either x = 22-30% or z = 3% was needed, and with y alone no clear liquid was obtained at all. For liquid B, neither x alone nor y alone nor z alone produced a clear liquid.

Claims (3)

I claim:
1. An aqueous built liquid detergent composition, consisting essentially of:
(a) 5-15% by weight of an anionic synthetic detergent selected from the group consisting of C10 -C24 alkylbenzene sulphonates, C10 -C24 alkane sulphonates and C10 -C24 alkylether sulphates containing 1-10 moles of ethylene- or propylene oxide;
(b) 1-5% by weight of a nonionic synthetic detergent selected from a group consisting of adducts of 5-30 moles of an alkylene oxide to C10 -C24 primary alcohols, C10 -C24 secondary alcohols, and C9 -C18 alkylphenols;
(c) 1-5% by weight of a sodium or potassium salt of dimerized oleic acid;
(d) 1-25% by weight of a sodium or potassium builder salt selected from the group consisting of orthophosphates, pyrophosphates, tripolyphosphates, carbonates and mixtures thereof;
(e) 0.75-8.5% by weight of an alkali metal or ammonium salt of xylene-, toluene- or cumene sulphonic acid;
(f) 0.5-2.5% by weight of a monoalkane phosphonic acid, in which the alkane group contains 4-10 carbon atoms, or the alkali metal or ammonium salt thereof, whereby the amount of salt of xylene sulphonic acid is more than 4% by weight when the amount of the monoalkane phosphonic acid is 1% or less.
2. A composition according to claim 1, further comprising 0.5-5% by weight of a sodium or potassium polyacrylate with a molecular weight of 3,500-22,000.
3. A composition according to claim 1, wherein the monoalkane phosphonic acid is monooctane phosphonic acid.
US05/773,863 1976-03-11 1977-03-03 Built liquid detergent composition Expired - Lifetime US4126572A (en)

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CA (1) CA1082559A (en)
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FR (1) FR2343806A1 (en)
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Cited By (11)

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US4446043A (en) * 1981-09-01 1984-05-01 Lever Brothers Company Built liquid detergent compositions
US4452717A (en) * 1980-04-09 1984-06-05 Lever Brothers Company Built liquid detergent compositions and method of preparation
US4560493A (en) * 1982-11-04 1985-12-24 Henkel Kommanditgesellschaft Auf Aktien Liquid residue reducing preparations containing octane-1-phosphonic acid or a water-soluble salt thereof
US4582636A (en) * 1984-12-18 1986-04-15 Colgate-Palmolive Co. Concentrated homogeneous built liquid detergent composition
US4690779A (en) * 1983-06-16 1987-09-01 The Clorox Company Hard surface cleaning composition
US4803068A (en) * 1983-01-24 1989-02-07 Henkel Kommanditgesellschaft Auf Aktien Hair-treatment preparation for improved wet combability
US4891148A (en) * 1985-08-05 1990-01-02 Colgate-Palmolive Company Low phosphate or phosphate free nonaqueous liquid nonionic laundry detergent comopsition and method of use
US5565141A (en) * 1992-05-11 1996-10-15 Basf Aktiengesellschaft Solubilizer mixture for the preparation of strongly alkaline aqueous solutions of non-ionic surfactants
KR100524132B1 (en) * 2001-07-19 2005-10-26 스타비루스 게엠베하 Arresting device between relative to each other moving two assemblies
US20080108537A1 (en) * 2006-11-03 2008-05-08 Rees Wayne M Corrosion inhibitor system for mildly acidic to ph neutral halogen bleach-containing cleaning compositions
WO2016177563A1 (en) 2015-05-07 2016-11-10 Unilever N.V. Alkaline dishwash composition

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Publication number Priority date Publication date Assignee Title
JPS58204099A (en) * 1982-05-25 1983-11-28 花王株式会社 liquid cleaning composition
DE3240688A1 (en) * 1982-11-04 1984-05-30 Henkel KGaA, 4000 Düsseldorf USE OF ALKYLMONOPHOSPHONIC ACIDS AS A KILLING SUBSTANCE
JP2691585B2 (en) * 1988-10-18 1997-12-17 花王株式会社 Alkaline cleaner

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US3122508A (en) * 1960-07-28 1964-02-25 Gen Aniline & Film Corp Heavy duty detergent compositions
US3156655A (en) * 1960-08-02 1964-11-10 Lever Brothers Ltd Heavy duty liquid detergent composition
US3630934A (en) * 1967-02-01 1971-12-28 Cincinnati Milacron Inc Mildness additive
US4021376A (en) * 1972-05-17 1977-05-03 Lever Brothers Company Detergent compositions with nonphosphate builders containing two or more carboxyl groups

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Publication number Priority date Publication date Assignee Title
US2397422A (en) * 1945-03-24 1946-03-26 Monsanto Chemicals Esters of paraffin phosphonic acids
US3122508A (en) * 1960-07-28 1964-02-25 Gen Aniline & Film Corp Heavy duty detergent compositions
US3156655A (en) * 1960-08-02 1964-11-10 Lever Brothers Ltd Heavy duty liquid detergent composition
US3630934A (en) * 1967-02-01 1971-12-28 Cincinnati Milacron Inc Mildness additive
US4021376A (en) * 1972-05-17 1977-05-03 Lever Brothers Company Detergent compositions with nonphosphate builders containing two or more carboxyl groups

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4452717A (en) * 1980-04-09 1984-06-05 Lever Brothers Company Built liquid detergent compositions and method of preparation
US4446043A (en) * 1981-09-01 1984-05-01 Lever Brothers Company Built liquid detergent compositions
US4560493A (en) * 1982-11-04 1985-12-24 Henkel Kommanditgesellschaft Auf Aktien Liquid residue reducing preparations containing octane-1-phosphonic acid or a water-soluble salt thereof
US4803068A (en) * 1983-01-24 1989-02-07 Henkel Kommanditgesellschaft Auf Aktien Hair-treatment preparation for improved wet combability
US4690779A (en) * 1983-06-16 1987-09-01 The Clorox Company Hard surface cleaning composition
US4582636A (en) * 1984-12-18 1986-04-15 Colgate-Palmolive Co. Concentrated homogeneous built liquid detergent composition
US4891148A (en) * 1985-08-05 1990-01-02 Colgate-Palmolive Company Low phosphate or phosphate free nonaqueous liquid nonionic laundry detergent comopsition and method of use
US5565141A (en) * 1992-05-11 1996-10-15 Basf Aktiengesellschaft Solubilizer mixture for the preparation of strongly alkaline aqueous solutions of non-ionic surfactants
KR100524132B1 (en) * 2001-07-19 2005-10-26 스타비루스 게엠베하 Arresting device between relative to each other moving two assemblies
US20080108537A1 (en) * 2006-11-03 2008-05-08 Rees Wayne M Corrosion inhibitor system for mildly acidic to ph neutral halogen bleach-containing cleaning compositions
WO2016177563A1 (en) 2015-05-07 2016-11-10 Unilever N.V. Alkaline dishwash composition

Also Published As

Publication number Publication date
FR2343806B1 (en) 1980-08-22
JPS5923358B2 (en) 1984-06-01
FR2343806A1 (en) 1977-10-07
DE2710727A1 (en) 1977-09-22
JPS52135312A (en) 1977-11-12
CA1082559A (en) 1980-07-29
DE2710727C2 (en) 1985-11-21
GB1576412A (en) 1980-10-08
NL7701967A (en) 1977-09-13

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